1 to 25 of 28 QMS Jobs in London

Business Analyst/QMS Consultant – Quality Management System Project/ISO9001 £500 - £600 PD (Outside IR35) Overview: An excellent opportunity has arisen with a leading international shipping organisation, renowned for their commitment to excellence, innovation, and customer satisfaction. They are embarking on an ambitious project to implement a state-of … quality management practices and systems existing processes and identify areas for improvement and integration detailed process documentation and workflows and develop a robust Quality Management System tailored to the company's needs. the system aligns with ISO9001 standards and industry best practices. with IT and other departments to integrate the … QMS with existing systems (Dynamics) Project Planning and Management: the end-to-end project lifecycle for the Quality Management System implementation. detailed project plans, timelines, and resource allocation. with stakeholders to define project scope and objectives. ISO9001 Accreditation: and guide the company through the ISO9001 accreditation process. and implement policies more »

that all costs are considered. Providing routine internal commercial and progress reporting in accordance with management time requirements Maintain systems to see that Quality Management System ISO 9001 and 14001 are implemented. Progress all sales opportunities. Develop and pursue new and existing sales leads Ensure No Claims are made on more »

also be considered. At least five years of quality management experience and a track record of supporting businesses on their quality agenda. Experience in QMS implementation, HACCP and Trade Associations promoting good food quality business practice. A passion for delving deep to gather all the information available to support identifying more »

the following: Scientific, Technical and Professional To undertake work as you are assigned in compliance with current CPA/UKAS accreditation and TDL Quality Management System and H&S requirements. To adhere to all standard operating procedures at all times as relevant to the department in which you are working. more »

development. Ophthalmic Knowledge: Knowledge of the ophthalmic field. GMP Experience: At least 2 years of experience working within a GMP environment, familiar with local QMS systems and compliant with EU GMP/EMA/ICH standards. Specialized Cell Culture: Experience in the generation, culture, and/or GMP manufacturing of more »

Able to communicate effectively (written and verbal) Desirable Good keyboard skills Knowledge Essential H&S legislation and procedures Specialist knowledge in Clinical Biochemistry. Quality management system Detailed understanding of UKAS Desirable Knowledge of current requirements for training and career progression Qualifications Essential Registered with the Health & Care Professions Council (HCPC more »

provided comprehensive language and technology solutions to help our clients communicate and conduct business more effectively in a global marketplace. Equipped with a quality management system certified to both the ISO 9001:2008 and EN 15038:2006 standards, TransPerfect provides a full array of language and business support services, including more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

quality incidents, safety occurrences, and customer complaints, and implement corrective and preventive actions as necessary. Provide support during regulatory inspections, customer audits, and quality management system certifications. What you will need: Strong knowledge of QA methodologies, tools, and best practices including Part 145 Safety Management Systems. Extensive experience in quality more »

In this role you will be responsible for assisting with the documentation, inspections and assessments of processes and products to ensure compliance with the QMS and continuous improvement of high-end projects. This would suit an engineer from a manufacturing background looking for the opportunity to grow their career within more »

To conduct the administrative aspect of the Technical Department taking responsibility for the day-to-day management of some or all of the following; QMS, HACCP, Legislation, Customer Specifications, Raw material specification. · Technical kpi generation and interpretation, including, non-conformance, customer complaints, microbiological performance · Helping to develop and maintain change more »

applications Desirable Big data analysis, image analysis and software use Apps creation and maintenance and webpage design Experience of working within a quality management system Knowledge Essential Good knowledge of underlying physics principles at degree level Knowledge of a programming language or computer coding Statistical analysis Desirable Clinical use of more »

prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO 13485 quality management system and collaborate effectively with other engineers to support research and development initiatives and the overall project goal Better patient outcomes! What skills and experience more »

the team and with external partners. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required Experience Good understanding of communications, wiring systems and schematics or equivalent Experience with inspection and testing– C more »

radiographer with 1 year in treatment planning Experience of Planning Breast and Pelvis Planning Experience of Planning using Eclipse Working with in a Quality Management System Skills Essential Ability to use complex computerised TPS [equivalent to CAD] Highly developed physical accuracy and hand-eye coordination. Advanced keyboard skills. Good spatial more »

out risk assessments You will be working to local and industry procedures and to comply with industry codes of practice and the Company quality management system You will be required to travel up to 2 hours from your home address with periods of absence from home will be expected from more »

company procedures and policies to ensure smooth delivery of our service Producing reporting on time and to agreed standards Adhering to the companys quality management system and recycle correctly and responsibly Experience & Skills UK Driving Licence (required) Experience in electrical repair, maintenance, servicing & installations, preferably within the public sector A more »

employment as and when required. You will also receive a full company induction that will include many areas such as GDPR the DBF Quality Management System and all other systems and soft skills training. About the Company Leading the way in Customer Interaction & process management the company are an international more »

a Pharma client. This role is focusing on the quality side of things and you will have a background in managing compliance, experience of QMS and be able to conduct investigations around CAPA. Three direct reports 30% travel Client is a large pharmaceutical/life science company. Job purpose Provide … that meets Group Health and Safety policy and client EHS policy requirements where required. Take EMEA account responsibility for the client Quality Management System (QMS) where implemented in line with contract and scope of QMS Job profile: This is an important role which has wide exposure to management providing a more »

Work with Customer Success Team to deploy and maintain client solution environments & configuration. Provide Tier 2 support. Ensure compliance with CYTE Quality Management System (QMS), including training assignments. In order to perform this role, individuals must have the following qualifications, competencies and personal qualities: Bachelor’s degree, or equivalent, in more »

be able to hold their own within a QMS. The ideal candidate must have at least two years of experience in a Pharmaceutical Quality Management System and understand and be able to complete QMS activities including: Change control Deviations CAPA QMRs Recalls Returns Training The role involves: Review, update and … bona fide reviews, reviewing Technical Agreements etc. Requirements: Experience/knowledge in the following is useful – Sage, Outlook, Microsoft 365, import of pharmaceuticals, pharmaceutical QMS or PLPI would be useful but not essential. The company has a MIA for PLPI as well as a WDA with a single QMS, so more »

coordinating IMP supply and eventual closure and archiving of the trial To be responsible for ensuring the requirements of the production area's quality management system are maintained and developed as required by the MS(specials), MIA(IMP) licenses and NHS guidance. To deputise for the Senior Production Pharmacist - Clinical … in accordance with data integrity principles to be audit ready at all times. Governance and Quality To ensure that the Clinical Trial Pharmaceutical Quality Management system is maintained and developed in accordance with the MS(Specials) and MIA(IMP) license requirements and in response to changes in regulations and legislation. … quality and final product disposition from a production perspective in liaison with QA and the QP. To support and document change through the Quality Management System to both reduce risk and drive innovation in clinical trial activities and the overall clinical trials service. To ensure all changes to the Quality more »

Reception, external referrals and the pathology call centre Main duties of the job The post holder will be responsible for embedding the NWLP quality management system across all sites and departments within Pathology Support Services and will be expected to drive continuous improvement in quality. The Pathology Support Services Quality … a joint post with the Point of Care Testing management team and will therefore also involve the management and maintenance of the POCT quality management system and preparation for accreditation assessment for POCT devices in use within the customer Trusts of NWLP. About us Benefits include career development, flexible working more »

of audit reports for both internal and external auditors. Collaborate with the Head of GQA and the audit team to enhance the audit quality management system, actively participating in process improvements including QMS documentation updates. Maintain current awareness of the regulatory and pharmaceutical industry environment, influencing internal Business Partners and more »

We have an exciting opportunity for a Specialist Biomedical Scientist-Histopathology (NHS Band 6 equivalent) to join our Histopathology Department. This role is a based at our Harley Street location (W1G 7JL). We are also offering a competitive salary more »